Reaction of 1-Antipyryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones with N-Substituted and N-Unsubstituted 3-Amino-5,5-dimethylcyclohex-2-en-1-ones
Nucleophilic transformations of N-antipyryl-substituted 1H-pyrrole-2,3-diones by the action of enamines derived from dimedone as 1,3-C,N-binucleophiles afforded 1′-antipyryl-3′-aroyl-4′-hydroxy-6,6-dimethyl-6,7-dihydrospiro[indole-3,2′-pyrrole]-2,4,5′(1H,1′H,5H)-triones and 1′-antipyryl-1-aryl-3′-aroyl-4′-hydroxy-6,6-dimethyl-6,7-dihydrospiro[indole-3,2′-pyrrole]-2,4,5′(1H,1′H,5H)-triones.
Authors
- Е. С. Денисламова (ORCID: https://orcid.org/0000-0003-1220-3625)
- А. Н. Масливец (ORCID: https://orcid.org/0000-0001-7148-4450)
- V. A. Lyadov (ORCID: https://orcid.org/0000-0002-7267-7577)
Institutions
- Perm State University (RU)
- Perm National Research Polytechnic University (RU)
Publication Details
- Journal
- Russian Journal of Organic Chemistry
- Published
- 2025-03-01
- DOI
- https://doi.org/10.1134/s1070428024603996
- Primary Topic
- Chemical synthesis and pharmacological studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00